SCHEMBL720142

SCHEMBL720142

O=C(c1ccc(F)cc1)c1ccc(-c2ccc(O)cc2)cc1

nearest known ligand 0.67

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
LMNA P02545 2/20 0.67
MAPT P10636 2/20 0.67
MEN1 O00255 1/20 0.67
RAB9A P51151 1/20 0.67
KMT2A Q03164 1/20 0.67
ESR1 P03372 3/20 0.65
ESR2 Q92731 1/20 0.65
PKM P14618 1/20 0.65
HPGD P15428 1/20 0.65
HTT P42858 1/20 0.65
BCL2L1 Q07817 1/20 0.59
BAD Q92934 1/20 0.59
SRD5A2 P31213 1/20 0.56
LTA4H P09960 1/20 0.55
NPC1 O15118 1/20 0.55
RXFP1 Q9HBX9 1/20 0.55
HSD17B1 P14061 2/20 0.54
MAPK1 P28482 1/20 0.54
MMP2 P08253 1/20 0.53
MMP3 P08254 1/20 0.53

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
SCHEMBL10871402 1.00 LMNA (0.67) LMNAMAPTMEN1RAB9AKMT2A
Hydroquinone SCHEMBL10631077 0.93 LMNA (0.75) LMNAMAPTMEN1RAB9AKMT2A
SCHEMBL4382240 0.93 LMNA (0.75) LMNAMAPTMEN1RAB9AKMT2A
SCHEMBL10631127 0.93 LMNA (0.75) LMNAMAPTMEN1RAB9AKMT2A
SCHEMBL10631102 0.93 LMNA (0.75) LMNAMAPTMEN1RAB9AKMT2A
SCHEMBL145363 0.93 LMNA (0.75) LMNAMAPTMEN1RAB9AKMT2A
Hydroquinone SCHEMBL10635290 0.93 LMNA (0.75) LMNAMAPTMEN1RAB9AKMT2A
SCHEMBL10346409 0.91 LMNA (0.71) LMNAMAPTMEN1RAB9AKMT2A
SCHEMBL9814506 0.91 BCL2L1 (0.70) LMNAMAPTMEN1RAB9AKMT2A
SCHEMBL1864175 0.91 BCL2L1 (0.70) LMNAMAPTMEN1RAB9AKMT2A

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 36 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-10023692-B2 Method for the manufacture of poly(aryl ether ketone)s in the presence of sodium carbonate SOLVAY ADVANCED POLYMERS, L.L.C. (US) 2018-07-17 US disclosed
EP-3147304-A1 POLYMERIC MATERIALS Victrex Manufacturing Limited (GB) 2017-03-29 EP disclosed
EP-3144336-A1 POLYMERIC MATERIALS Victrex Manufacturing Limited (GB) 2017-03-22 EP disclosed
US-20160145385-A1 METHOD FOR THE MANUFACTURE OF POLY(ARYL ETHER KETONE)S IN THE PRESENCE OF SODIUM CARBONATE SOLVAY ADVANCED POLYMERS, L.L.C. (US) 2016-05-26 US disclosed
US-9175136-B2 Method for the manufacture of poly(aryl ether ketone)s in the presence of sodium carbonate SOLVAY ADVANCED POLYMERS, L.L.C. (US) 2015-11-03 US disclosed
US-20140128566-A1 POLYMERIC MATERIALS VICTREX MANUFACTURING LIMITED (GB) 2014-05-08 US disclosed
EP-2344565-B1 METHOD FOR THE MANUFACTURE OF POLY(ARYL ETHER KETONE)S IN THE PRESENCE OF SODIUM CARBONATE SOLVAY SPECIALTY POLYMERS USA (US) 2014-03-19 EP disclosed
US-8445141-B2 Sulfonic acid group-containing polymer, method for producing the same, resin composition containing such sulfonic acid group-containing polymer, polymer electrolyte membrane, polymer electrolyte membrane/electrode assembly, and fuel cell TOYO BOSEKI KABUSHIKI KAISHA (JP) 2013-05-21 US disclosed
US-8216727-B2 Aromatic hydrocarbon based proton exchange membrane and direct methanol fuel cell using same TOYO BOSEKI KABUSHIKI KAISHA (JP) 2012-07-10 US disclosed
US-20120052411-A9 AROMATIC HYDROCARBON BASED PROTON EXCHANGE MEMBRANE AND DIRECT METHANOL FUEL CELL USING SAME TOYO BOSEKI KABUSHIKI KAISHA (JP) 2012-03-01 US disclosed
EP-1561768-A1 POLYARYLENE ETHER COMPOUND CONTAINING SULFONIC ACID GROUP, COMPOSITION CONTAINING SAME, AND METHOD FOR MANUFACTURING THOSE Toyo Boseki Kabushiki Kaisha (JP) 2005-08-10 EP disclosed
US-4999414-A Process for the production of aromatic polyether ketones BAYER AKTIENGESELLSCHAFT (DE) 1991-03-12 US disclosed
EP-0193187-B1 PROCESS FOR PREPARING CRYSTALLINE AROMATIC POLYETHERKETONES Asahi Kasei Kogyo Kabushiki Kaisha (JP) 1990-06-13 EP disclosed
EP-0354377-A2 Process for the preparation of aromatic polyether ketones BAYER AG (DE) 1990-02-14 EP disclosed
US-4868273-A SOLVENT RESISTANT POLYETHERS CONTAINING SULFONE AND CARBONYL GROUPS IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1989-09-19 US disclosed
EP-0303389-A2 Aromatic polymer IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1989-02-15 EP disclosed
US-4777300-A Aromatic ketone IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1988-10-11 US disclosed
US-4757126-A Polycondensing 4,4'-dihydroxybenzophenone or hydroquinone with dihalogenoaromatic ketone in solvent in the presence of an alkali ASAHI KASEI KOGYO KABUSHIKI KAISHA (JP) 1988-07-12 US disclosed
EP-0232019-A2 Aromatic Polymer IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1987-08-12 EP disclosed
EP-0193187-A1 Process for preparing crystalline aromatic polyetherketones Asahi Kasei Kogyo Kabushiki Kaisha (JP) 1986-09-03 EP disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (1 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-10023692-B2 Method for the manufacture of poly(aryl ether ketone)s in the presence of sodium carbonate PKM, KCNK10, KCNK9 LMNA 1173/4885MAPT 3336/4885MEN1 4737/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.